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猛禽中检测到的一种新型腺病毒的确认:部分序列及系统发育分析

Confirmation of a novel siadenovirus species detected in raptors: partial sequence and phylogenetic analysis.

作者信息

Kovács Endre R, Benko Mária

机构信息

Veterinary Medical Research Institute, Hungarian Academy of Sciences, P.O. Box 18, H-1581 Budapest, Hungary.

出版信息

Virus Res. 2009 Mar;140(1-2):64-70. doi: 10.1016/j.virusres.2008.11.005. Epub 2008 Dec 18.

Abstract

Partial genome characterisation of a novel adenovirus, found recently in organ samples of multiple species of dead birds of prey, was carried out by sequence analysis of PCR-amplified DNA fragments. The virus, named as raptor adenovirus 1 (RAdV-1), has originally been detected by a nested PCR method with consensus primers targeting the adenoviral DNA polymerase gene. Phylogenetic analysis with the deduced amino acid sequence of the small PCR product has implied a new siadenovirus type present in the samples. Since virus isolation attempts remained unsuccessful, further characterisation of this putative novel siadenovirus was carried out with the use of PCR on the infected organ samples. The DNA sequence of the central genome part of RAdV-1, encompassing nine full (pTP, 52K, pIIIa, III, pVII, pX, pVI, hexon, protease) and two partial (DNA polymerase and DBP) genes and exceeding 12 kb pairs in size, was determined. Phylogenetic tree reconstructions, based on several genes, unambiguously confirmed the preliminary classification of RAdV-1 as a new species within the genus Siadenovirus. Further study of RAdV-1 is of interest since it represents a rare adenovirus genus of yet undetermined host origin.

摘要

通过对聚合酶链反应(PCR)扩增的DNA片段进行序列分析,对最近在多种死亡猛禽的器官样本中发现的一种新型腺病毒进行了部分基因组特征分析。该病毒被命名为猛禽腺病毒1型(RAdV-1),最初是通过一种巢式PCR方法检测到的,该方法使用靶向腺病毒DNA聚合酶基因的共有引物。对小PCR产物推导的氨基酸序列进行系统发育分析,表明样本中存在一种新的禽腺病毒类型。由于病毒分离尝试未成功,因此利用PCR技术对受感染的器官样本进行进一步分析,以鉴定这种假定的新型禽腺病毒。确定了RAdV-1中心基因组部分的DNA序列,其包含9个完整基因(pTP、52K、pIIIa、III、pVII、pX、pVI、六邻体、蛋白酶)和2个部分基因(DNA聚合酶和DBP),大小超过12千碱基对。基于多个基因重建的系统发育树明确证实了RAdV-1作为禽腺病毒属内一个新物种的初步分类。对RAdV-1的进一步研究很有意义,因为它代表了一种宿主来源尚未确定的罕见腺病毒属。

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